Chinese Journal of Tissue Engineering Research ›› 2018, Vol. 22 ›› Issue (14): 2168-2173.doi: 10.3969/j.issn.2095-4344.0743

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Effects of collagen-bioactive glass-polycaprolactone scaffold on proliferation, migration and differentiation of human dental pulp cells

Pan Fu-qin1, Liu Jian-hui2, Pang Yin2, Qiu Yan-li1, Zhou Jing1, Li Qi1, Cai Chun-yi3   

  1. 1Department of Stomatology, 2Department of Anatomy, Cangzhou Medical College, Cangzhou 061001, Hebei Province, China; 3Department of Pathology, Cangzhou People’s Hospital, Cangzhou 061001, Hebei Province, China
  • Received:2017-12-01 Online:2018-05-18 Published:2018-05-18
  • Contact: Liu Jian-hui, Lecturer, Department of Anatomy, Cangzhou Medical College, Cangzhou 061001, Hebei Province, China
  • About author:Pan Fu-qin, Master, Lecturer, Attending physician, Department of Stomatology, Cangzhou Medical College, Cangzhou 061001, Hebei Province, China

Abstract:

BACKGROUND: Collagen-bioglass-polycaprolacton (COL-BG-PCL) composites have good biocompatibility, mechanical properties and biodegradability that are beneficial to cell adhesion, proliferation and angiogenesis.

OBJECTIVE: To study the effect of COL-BG-PCL bioactive scaffold on the proliferation, migration and differentiation of human dental pulp cells (hDPCs).
METHODS: hDPCs were isolated and cultured on the COL-BG-PCL bioactive scaffold. MTT, cell scratch test and enzyme-linked immunosorbent assay (ELISA) assay were used to detect the proliferation, migration and differentiation abilities of hDPCs before and at 1, 3, 7, 14, 24 days after inoculation onto the COL-BG-PCL bioactive scaffold.
RESULTS AND CONCLUSION: Compared with the cells without inoculation onto the COL-BG-PCL bioactive scaffold, (1) the proliferation ability of the cells cultured on the COL-BG-PCL scaffold was significantly enhanced (P < 0.01), and with the prolongation of the inoculation time, the cell proliferation ability was gradually increased; (2) the cell migration ability of the cells cultured on the COL-BG-PCL scaffold was significantly enhanced (P < 0.01), and with the prolongation of the inoculation time, the migration ability of the cells cultured on the COL-BG-PCL scaffold was gradually increased; (3) the level of alkaline phosphatase in the supernatant of the cells cultured on the COL-BG-PCL scaffold was significantly increased (P < 0.01), and with the prolongation of the inoculation time, the level of alkaline phosphatase in the supernatant was gradually increased. In summary, the COL-BG-PCL scaffold can promote the proliferation, migration and differentiation of hDPCs. 

Key words: Fibroblasts, Collagen, Cell Proliferation, Tissue Engineering

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